CA2787905A1 - Preparing ether carboxylates - Google Patents
Preparing ether carboxylates Download PDFInfo
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- CA2787905A1 CA2787905A1 CA2787905A CA2787905A CA2787905A1 CA 2787905 A1 CA2787905 A1 CA 2787905A1 CA 2787905 A CA2787905 A CA 2787905A CA 2787905 A CA2787905 A CA 2787905A CA 2787905 A1 CA2787905 A1 CA 2787905A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/23—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups
- C07C51/235—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups of —CHO groups or primary alcohol groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/295—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with inorganic bases, e.g. by alkali fusion
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/235—Saturated compounds containing more than one carboxyl group
- C07C59/305—Saturated compounds containing more than one carboxyl group containing ether groups, groups, groups, or groups
Abstract
The invention relates to a method for producing ether carboxylates.
Description
Preparing ether carboxylates The present invention relates to a process for preparing ether carboxylates.
Ether carboxylates are typically prepared in a batch operation, normally by initially charging the alkxoylate, a base such as NaOH and a catalyst such as Raney copper and bringing this reaction mixture to reaction temperature under superatmospheric pressure.
The class of ether carboxylates, useful as mild anionic surfactants, is long known.
US 2,183,853, having a 1934 priority date, describes preparing ether carboxylates by reacting alkoxylates with sodium and sodium chloroacetate at temperatures between 160 and 200 C. To achieve high conversions and low by-product formation, it is described as advantageous to add the base and chloroacetic acid at different points of the reactor with stirring. To remove resulting or added water from the reaction solution and to achieve a very quick reaction, the reaction is carried out at 70 to 90 C and a pressure of about 10 to 50 mbar.
DE 31 35 946 describes the direct oxidation of the alkoxylates with oxygen or oxygen-containing gases in an aqueous alkali medium over a platinum or palladium catalyst as a further way of preparing ether carboxylates.
The oxidative dehydrogenation of alcohols to carboxylates by thermal reaction of the alcohol with alkali metals or alkali metal hydroxides has been known since (Dumas and Stag, Ann, 35, 129 to 173). This reaction was classically carried out without catalyst and at > 200 C. US 2,384,818, issued 1945, employs this method for oxidizing amino alcohols.
Similarly, the use of catalysts for the oxidative dehydrogenation is long known.
US 2,384,817, filed 1942, describes the positive influence of cadmium, copper, nickel, silver, lead and zinc compounds on the reaction rate.
EP 0 620 209 describes a process to manufacture carboxylic acid salts by contacting an aqueous solution of a primary alcohol with an alkali metal hydroxide in the presence of an effective amount of a specific and activated Raney copper catalyst containing from 50 to 10 000 ppm of an element selected from the group consisting of chromium, titanium, niobium, tantalum, zirconium, vanadium, molybdenum, manganese, tungsten, cobalt and mixtures thereof, or from 50 to 10 000 ppm of nickel. The alcohol may be aliphatic, aromatic or a polyol. It is stated that both the alcohol - which necessarily will have a certain solubility in water - and the resulting carboxylate have to be stable in the hot and caustic solution. In addition, superatmospheric pressure is necessary for the reaction in order that the reaction temperatures described may be attained.
Amino alcohols, aromatic alcohols and ethylene glycol are recited as examples.
Ether carboxylates are typically prepared in a batch operation, normally by initially charging the alkxoylate, a base such as NaOH and a catalyst such as Raney copper and bringing this reaction mixture to reaction temperature under superatmospheric pressure.
The class of ether carboxylates, useful as mild anionic surfactants, is long known.
US 2,183,853, having a 1934 priority date, describes preparing ether carboxylates by reacting alkoxylates with sodium and sodium chloroacetate at temperatures between 160 and 200 C. To achieve high conversions and low by-product formation, it is described as advantageous to add the base and chloroacetic acid at different points of the reactor with stirring. To remove resulting or added water from the reaction solution and to achieve a very quick reaction, the reaction is carried out at 70 to 90 C and a pressure of about 10 to 50 mbar.
DE 31 35 946 describes the direct oxidation of the alkoxylates with oxygen or oxygen-containing gases in an aqueous alkali medium over a platinum or palladium catalyst as a further way of preparing ether carboxylates.
The oxidative dehydrogenation of alcohols to carboxylates by thermal reaction of the alcohol with alkali metals or alkali metal hydroxides has been known since (Dumas and Stag, Ann, 35, 129 to 173). This reaction was classically carried out without catalyst and at > 200 C. US 2,384,818, issued 1945, employs this method for oxidizing amino alcohols.
Similarly, the use of catalysts for the oxidative dehydrogenation is long known.
US 2,384,817, filed 1942, describes the positive influence of cadmium, copper, nickel, silver, lead and zinc compounds on the reaction rate.
EP 0 620 209 describes a process to manufacture carboxylic acid salts by contacting an aqueous solution of a primary alcohol with an alkali metal hydroxide in the presence of an effective amount of a specific and activated Raney copper catalyst containing from 50 to 10 000 ppm of an element selected from the group consisting of chromium, titanium, niobium, tantalum, zirconium, vanadium, molybdenum, manganese, tungsten, cobalt and mixtures thereof, or from 50 to 10 000 ppm of nickel. The alcohol may be aliphatic, aromatic or a polyol. It is stated that both the alcohol - which necessarily will have a certain solubility in water - and the resulting carboxylate have to be stable in the hot and caustic solution. In addition, superatmospheric pressure is necessary for the reaction in order that the reaction temperatures described may be attained.
Amino alcohols, aromatic alcohols and ethylene glycol are recited as examples.
EP 1 125 633 describes the use of doped Raney copper (doped with at least one element from the iron group or with a precious metal), the inactivation of which by agglomeration is distinctly reduced and the use cycles are therefore higher.
The invention relates to the preparation of carboxylic acids from alcohols. Again, the oxidative dehydrogenation of diethanolamine under strongly basic conditions at and 10 bar pressure is given as an example. The alcohols have to be soluble in water and the alcohol and also the carboxylic acid have to be stable to the strongly basic solution.
EP 1 125 634 describes a Raney copper fixed bed catalyst (with doping from iron or a precious metal), its simple filterability from the reaction solution and its use in the context of a continuous process. It is stated to be a prerequisite for the reaction of the alcohols that both the reactant and the product have to be stable in the strongly basic solutions and the alcohol has to be soluble in water.
US 5,916,840 describes preparing carboxylic acid salts in the presence of a supported catalyst consisting of an alkali-resistant support material (activated carbon for example), an anchor metal (palladium for example) and a discretely applied active metal (copper for example). The reaction takes place in a batch autoclave in the presence of water at 160 to 170 C. Continuing this principle, WO 03/033140 describes further catalysts for preparing iminodiacetic acid from diethanolamine. The preferred reaction condition is said to be the use of alkali metal hydroxides (equimolar use), use of a solvent and of a catalyst (at least 1% by mass) at temperatures of 120 to under superatmospheric pressure.
WO 98/13140 describes a catalyst for dehydrogenation of amino alcohols and ethylene glycol derivatives, consisting of zirconium, copper and optionally a further metal. The reaction of ethylene glycols such as triethylene glycol with 1 eq of NaOH in aqueous solution at 180 C and 10 bar pressure over the described catalyst (30% by mass) is disclosed.
US 4,110,371 describes a process for preparing dicarboxylic acid salts from compounds consisting of 2 to 6 ethylene glycol units with aqueous alkali metal hydroxide solution at temperatures of 200 to 300 C using a catalyst consisting of nickel, copper and chromium.
US 3,717,676 describes a method of preparing alkali metal salts of oxypolycarboxylates wherein an oxysubstituted or polyoxysubstituted primary alcohol is reacted with alkali metal hydroxide, 20% to 60% of water at 190 to 230 C, a pressure of 7 to 14 bar over a cadmium catalyst.
The invention relates to the preparation of carboxylic acids from alcohols. Again, the oxidative dehydrogenation of diethanolamine under strongly basic conditions at and 10 bar pressure is given as an example. The alcohols have to be soluble in water and the alcohol and also the carboxylic acid have to be stable to the strongly basic solution.
EP 1 125 634 describes a Raney copper fixed bed catalyst (with doping from iron or a precious metal), its simple filterability from the reaction solution and its use in the context of a continuous process. It is stated to be a prerequisite for the reaction of the alcohols that both the reactant and the product have to be stable in the strongly basic solutions and the alcohol has to be soluble in water.
US 5,916,840 describes preparing carboxylic acid salts in the presence of a supported catalyst consisting of an alkali-resistant support material (activated carbon for example), an anchor metal (palladium for example) and a discretely applied active metal (copper for example). The reaction takes place in a batch autoclave in the presence of water at 160 to 170 C. Continuing this principle, WO 03/033140 describes further catalysts for preparing iminodiacetic acid from diethanolamine. The preferred reaction condition is said to be the use of alkali metal hydroxides (equimolar use), use of a solvent and of a catalyst (at least 1% by mass) at temperatures of 120 to under superatmospheric pressure.
WO 98/13140 describes a catalyst for dehydrogenation of amino alcohols and ethylene glycol derivatives, consisting of zirconium, copper and optionally a further metal. The reaction of ethylene glycols such as triethylene glycol with 1 eq of NaOH in aqueous solution at 180 C and 10 bar pressure over the described catalyst (30% by mass) is disclosed.
US 4,110,371 describes a process for preparing dicarboxylic acid salts from compounds consisting of 2 to 6 ethylene glycol units with aqueous alkali metal hydroxide solution at temperatures of 200 to 300 C using a catalyst consisting of nickel, copper and chromium.
US 3,717,676 describes a method of preparing alkali metal salts of oxypolycarboxylates wherein an oxysubstituted or polyoxysubstituted primary alcohol is reacted with alkali metal hydroxide, 20% to 60% of water at 190 to 230 C, a pressure of 7 to 14 bar over a cadmium catalyst.
JP 10 277 391 finally describes the use of ultra-fine copper catalysts having particle sizes of 1 to 20 microns for preparing alkyl ether carboxylates from polyoxyethylene alkyl ethers and their use as an anionic surfactant in soap and cosmetic applications.
The fine state of subdivision of the catalyst gives a distinctly higher activity than classic Raney copper or copper-zirconium catalysts (comparative example involving Raney copper from Degussa shows a conversion of merely 15% instead of 98% under otherwise equivalent conditions).
The processes described accordingly all have a number of disadvantages which it has proved impossible to overcome despite the many years of research in this field. A
combination of pressure, high temperatures and strongly alkaline conditions is as ever required, imposing a severe stress on the material used (stress corrosion cracking), limiting reactivity as well as selectivity, the catalysts used are costly since they have to be inconveniently doped and form clumps during the process; only water-soluble and hence frequently rather short-chain alcohols can be used; moreover, the alcohol used and the product formed have to be base-resistant; and vinyl ethers, frequently formed as scissioning products, are not wanted in the product formed, yet are very difficult to detect analytically.
It is an object of the present invention to provide a process that reduces and/or eliminates the disadvantages mentioned.
We have found that this object is achieved, surprisingly, by a process for preparing an ether carboxylate of formula I
O p M
O' Wn R4 R2 4~_ R2 R2 IR4 1 RO O\ ]~X'X (" /o I J~ oM1 O p ( m 0 n Rl ~ ~lt O ,n` ~ Jm~L`' O p 9 comprising reacting the corresponding alkoxylate of formula II
The fine state of subdivision of the catalyst gives a distinctly higher activity than classic Raney copper or copper-zirconium catalysts (comparative example involving Raney copper from Degussa shows a conversion of merely 15% instead of 98% under otherwise equivalent conditions).
The processes described accordingly all have a number of disadvantages which it has proved impossible to overcome despite the many years of research in this field. A
combination of pressure, high temperatures and strongly alkaline conditions is as ever required, imposing a severe stress on the material used (stress corrosion cracking), limiting reactivity as well as selectivity, the catalysts used are costly since they have to be inconveniently doped and form clumps during the process; only water-soluble and hence frequently rather short-chain alcohols can be used; moreover, the alcohol used and the product formed have to be base-resistant; and vinyl ethers, frequently formed as scissioning products, are not wanted in the product formed, yet are very difficult to detect analytically.
It is an object of the present invention to provide a process that reduces and/or eliminates the disadvantages mentioned.
We have found that this object is achieved, surprisingly, by a process for preparing an ether carboxylate of formula I
O p M
O' Wn R4 R2 4~_ R2 R2 IR4 1 RO O\ ]~X'X (" /o I J~ oM1 O p ( m 0 n Rl ~ ~lt O ,n` ~ Jm~L`' O p 9 comprising reacting the corresponding alkoxylate of formula II
OH
Jp M
OJnL
RO 0 O\1 X( /OH1 p mL O ~nl Rl J LT O 1nl 1 Jm~ O lp q where independently R1 is a C1- to C5o-alkyl, mono-, di-, tri-,...polyamine, Xis O, COO, CH2-NH-O for r = 0 and q = 1 or N, C -N , N(CH2)tO for r = 0 to 50 and q = 2, r is an integer from 0 to 50, R2 is H or C r to Cio-alkyl, R3 is H or Cr to C,o-alkyl, R4 is H or C,- to C,o-alkyl, M is H or a metal, preferably alkali, alkaline earth, ammonium, organic base, n is from 0 to 50, m is from 0 to 40, p is from 0 to 40, q is from 1 to 20, s is 0 or 1, t is from 0 to 20, provided that n + m + p is at least 1 and R is C,- to C5o-alkyl, C1- to C5o-alkenyl, C,- to C5o-alkynyl, C6- to C5o-aryl, C6- to C5o-alkylaryl, H or a metal, preferably alkali, alkaline earth, with a base by using a transition metal catalyst, the base being added to the reaction mixture discontinuously at two or more times or continuously over a period above 30 minutes.
There are various preferred embodiments; in one, when s is 0, R is C,- to C5o-alkyl, Cl- to C50-alkenyl, C,- to C5o-alkynyl, C6- to C5o-aryl or C6- to C50-alkylaryl;
in the other, when s is 1, R is H or a metal, preferably alkali, alkaline earth.
There are also preferred ranges for r. r is preferably from 1 to 20 and more preferably from 2 to 10.
Preference is given to a process for preparing an ether carboxylate of formula III
~X~ f 0 OM J
R Lam' 0~ m O~ q comprising reacting the corresponding alkoxylate of formula IV
R ~T" 0~ m O_ Jp q 5 where independently R is Cl- to C5o-alkyl, Cl- to C5o-alkenyl, Cl- to C5o-alkynyl, C6- to C5o-aryl, C6- to C5o-alkylaryl, H or a metal, preferably alkali, alkaline earth, X is O, COO, CH2-NH-O for q = 1 or N, C -N, N(CH2)1O for q = 2 R2 is H or Cr to C io-alkyl, R3 is H or C,- to C,o-alkyl, R4 is H or Cr to C,o-alkyl, M is H or a metal, preferably alkali, alkaline earth, ammonium, organic base, n is from 0 to 50, m is from 0 to 40, p is from 0 to 40, q is from 1 to 2, t is from 1 to 10, provided that n + m + p is at least 1, with a base by using a transition metal catalyst, the base being added to the reaction mixture discontinuously at two or more times or continuously over a period above 30 minutes.
A process for preparing an ether carboxylate of formula V
OM
~1 L R3 0 V
comprising reacting the corresponding alkoxylate of formula VI
~X/O~}~J /OH
R O n Jm~ O JP
where independently R is C,- to C5o-alkyl, Cl- to C5o-alkenyl, Cl- to C5o-alkynyl, C6- to C5o-aryl, C6- to C5o-alkylaryl, H or a metal, preferably alkali, alkaline earth, XisO, R2 is H or C1- to C1o-alkyl, R3 is H or Cr to C1o-alkyl, R4 is H or C1- to C1o-alkyl, n is from 0 to 50, m is from 0 to 40, p is from 0 to 40, preferably from 1 to 20 and more preferably from 5 to 10, provided that n + m + p is at least 1, with a base by using a transition metal catalyst, the base being added to the reaction mixture discontinuously at two or more times or continuously over a period above 30 minutes.
There are preferred versions with regard to the alkoxylates used so that a process is preferred wherein independently R is C1- to Cso-alkyl, C1- to Cso-alkenyl, Cl- to C5o-alkynyl, C6- to C5o-aryl, C6- to C5o-alkylaryl, H or a metal, preferably alkali, alkaline earth, Xis0, R2 is H or C2- to C8-alkyl, R3 is H or C2- to C8-alkyl, R4 is H or C2- to C8-alkyl, n is from 1 to 30, m is from 1 to 20, p is from 1 to 20, n + m + p is atleast2.
Particular preference is given to a process wherein independently X is 0 or COO, R is C2- to C1o-alkyl, R2 is H or C3- to C5-alkyl, R3 is H or C3- to C6-alkyl, R4 is H or C3- to C6-alkyl, n is from 1 to 18, m is from 1 to 12, m is from 1 to 12, n+m+pis at least 5.
R is more particularly methyl, ethyl, propyl, butyl, pentyl, hexyl, octyl, 2-ethylhexyl and 2-propylheptyl, dodecyl, tridecyl, myristyl, lauryl, i-C17, tall oil fat (C16,18), behenyl.
R2, R3 and R4, if present, are each more particularly and independently hydrogen, methyl, ethyl, propyl, butyl, pentyl and isobutyl, of which hydrogen, methyl and ethyl are particularly preferred and methyl and ethyl are very particularly preferred.
n is most preferably in the range from 3 to 20.
m is more preferably in the range from 3 to 20.
p is more preferably in the range from 3 to 20.
The sum total of n, m and p is more preferably in the range from 3 to 20. The individual alkoxide units can be arranged in various ways, for example randomly, in block form or with a gradient. Particular preference is given to processes first using a higher oxide, for example propylene oxide, and then EO.
In addition to various alkylene oxides, the process of the present invention may also utilize various alkoxylates a, b, c, ..., z being added at one or more times.
For instance, compounds where Ra = C12,14 to C2o and Rb = C2 to C10 may be used with advantage.
A useful base is in principle any compound capable of deprotonating the alkoxylate used. This includes bases within the meaning of Bjerrum's acid-base definition. There are certain preferred bases and hence a process wherein the base is selected from the group consisting of NaOH, KOH, Mg(OH)2, Ca(OH)2, ammonium hydroxide, choline hydroxide and hydrotalcite constitutes a particularly preferred embodiment of the present invention. Hydrotalcite is particularly preferred when the product is to have narrow molar mass distributions.
The base is added to the reaction mixture during the reaction either batchwise or continuously. This means that the base, or portions of the base, are added to the reaction mixture at a time at which reaction conditions are present.
A preferred embodiment is accordingly a process wherein the base is added to the reaction mixture at 2 to 10 000 times. The number of times at which the base is added is preferably in the range from 3 to 1000, more preferably in the range from 4 to 100 and most preferably in the range from 5 to 20.
Another preferred embodiment is a process wherein the base is added to the reaction mixture over a period of more than 30 minutes. The period over which the base is added to the reaction mixture is particularly advantageous in the range from more than 2 h to 10 h, preferably in the range from 5 h to 9 h and even more preferably in the range from 6 h to 8 h.
In both cases, i.e., in the case of the continuous addition of the base and in the case of the batchwise addition of the base, the base can be introduced into the reaction mixture at various places. It is particularly preferable when the base is added to the reactor at 2 to 10 places and preferably at 3 to 5 places. This procedure can be used to reduce the local concentration of base in the reaction mixture still further and thereby further suppress the formation of by-products.
As far as the catalyst is concerned, the metals of groups 4 to 12, i.e., from Ti to Zn and those thereunder, come into consideration as both main and secondary constituent, those of groups 8 to 11, i.e., Fe - Cu and those thereunder, being preferred.
And it is accordingly the case that a process wherein the transition metal catalyst comprises at least one metal selected from the group consisting of Fe, Cu, Co and Ni is preferred.
The transition metal can be in a variety of forms, such as pure metal or as metal oxide, but it is preferably present in activated form, as Raney metal. Raney copper is particularly preferred. This Raney copper can also be still further modified, for example by doping with other metals. It is an advantage of the process of the present invention that such doping is not needed to achieve a good result for the synthesis, but it may nevertheless be advantageous to further improve the result of the synthesis.
The preparation of suitable transition metal catalysts is described for example in EP 1 125 634 (Degussa), where a simple Raney copper fixed bed catalyst is disclosed.
EP 1 125 633 (Degussa) describes Raney copper comprising various dopants [example: 1 % Pt, 3% Fe, 2000 ppm Cr or 1 % V on Raney Cu], and it is shown that the doped catalysts deactivate less than conventional Raney copper (Degussa BFX
3113W). WO 96/01146 (Monsato) finally describes C support with a precious metal, for example Pt applied as anchor metal on the Cu. This technique is stated to likewise prevent the sintering of the Cu. A particularly preferred combination of transition metals is that of copper and iron. DMC catalysts are more particularly preferred.
The present process leaves only small amounts of catalyst in the product. In a preferred process the M content of the product is in the range from 0.1 ppm to 1%, preferably in the range from 1 to 500 ppm and more preferably in the range from 10 to 50 ppm.
The process of the present invention can pleasingly also be carried out on a large scale. Preference is accordingly given to a process utilizing more than 1 kg, preferably more than 10 kg, even more preferably more than 100 kg and most preferably more than 1 t (metric ton) of alkoxylate.
The process of the present invention wherein the reaction temperature is in the range from 140 C to 220 C is preferred. More preference is given to processes carried out in the temperature range from 160 to 200 C and more particularly in the range from 160 to 190 C, for example at 180 C.
Jp M
OJnL
RO 0 O\1 X( /OH1 p mL O ~nl Rl J LT O 1nl 1 Jm~ O lp q where independently R1 is a C1- to C5o-alkyl, mono-, di-, tri-,...polyamine, Xis O, COO, CH2-NH-O for r = 0 and q = 1 or N, C -N , N(CH2)tO for r = 0 to 50 and q = 2, r is an integer from 0 to 50, R2 is H or C r to Cio-alkyl, R3 is H or Cr to C,o-alkyl, R4 is H or C,- to C,o-alkyl, M is H or a metal, preferably alkali, alkaline earth, ammonium, organic base, n is from 0 to 50, m is from 0 to 40, p is from 0 to 40, q is from 1 to 20, s is 0 or 1, t is from 0 to 20, provided that n + m + p is at least 1 and R is C,- to C5o-alkyl, C1- to C5o-alkenyl, C,- to C5o-alkynyl, C6- to C5o-aryl, C6- to C5o-alkylaryl, H or a metal, preferably alkali, alkaline earth, with a base by using a transition metal catalyst, the base being added to the reaction mixture discontinuously at two or more times or continuously over a period above 30 minutes.
There are various preferred embodiments; in one, when s is 0, R is C,- to C5o-alkyl, Cl- to C50-alkenyl, C,- to C5o-alkynyl, C6- to C5o-aryl or C6- to C50-alkylaryl;
in the other, when s is 1, R is H or a metal, preferably alkali, alkaline earth.
There are also preferred ranges for r. r is preferably from 1 to 20 and more preferably from 2 to 10.
Preference is given to a process for preparing an ether carboxylate of formula III
~X~ f 0 OM J
R Lam' 0~ m O~ q comprising reacting the corresponding alkoxylate of formula IV
R ~T" 0~ m O_ Jp q 5 where independently R is Cl- to C5o-alkyl, Cl- to C5o-alkenyl, Cl- to C5o-alkynyl, C6- to C5o-aryl, C6- to C5o-alkylaryl, H or a metal, preferably alkali, alkaline earth, X is O, COO, CH2-NH-O for q = 1 or N, C -N, N(CH2)1O for q = 2 R2 is H or Cr to C io-alkyl, R3 is H or C,- to C,o-alkyl, R4 is H or Cr to C,o-alkyl, M is H or a metal, preferably alkali, alkaline earth, ammonium, organic base, n is from 0 to 50, m is from 0 to 40, p is from 0 to 40, q is from 1 to 2, t is from 1 to 10, provided that n + m + p is at least 1, with a base by using a transition metal catalyst, the base being added to the reaction mixture discontinuously at two or more times or continuously over a period above 30 minutes.
A process for preparing an ether carboxylate of formula V
OM
~1 L R3 0 V
comprising reacting the corresponding alkoxylate of formula VI
~X/O~}~J /OH
R O n Jm~ O JP
where independently R is C,- to C5o-alkyl, Cl- to C5o-alkenyl, Cl- to C5o-alkynyl, C6- to C5o-aryl, C6- to C5o-alkylaryl, H or a metal, preferably alkali, alkaline earth, XisO, R2 is H or C1- to C1o-alkyl, R3 is H or Cr to C1o-alkyl, R4 is H or C1- to C1o-alkyl, n is from 0 to 50, m is from 0 to 40, p is from 0 to 40, preferably from 1 to 20 and more preferably from 5 to 10, provided that n + m + p is at least 1, with a base by using a transition metal catalyst, the base being added to the reaction mixture discontinuously at two or more times or continuously over a period above 30 minutes.
There are preferred versions with regard to the alkoxylates used so that a process is preferred wherein independently R is C1- to Cso-alkyl, C1- to Cso-alkenyl, Cl- to C5o-alkynyl, C6- to C5o-aryl, C6- to C5o-alkylaryl, H or a metal, preferably alkali, alkaline earth, Xis0, R2 is H or C2- to C8-alkyl, R3 is H or C2- to C8-alkyl, R4 is H or C2- to C8-alkyl, n is from 1 to 30, m is from 1 to 20, p is from 1 to 20, n + m + p is atleast2.
Particular preference is given to a process wherein independently X is 0 or COO, R is C2- to C1o-alkyl, R2 is H or C3- to C5-alkyl, R3 is H or C3- to C6-alkyl, R4 is H or C3- to C6-alkyl, n is from 1 to 18, m is from 1 to 12, m is from 1 to 12, n+m+pis at least 5.
R is more particularly methyl, ethyl, propyl, butyl, pentyl, hexyl, octyl, 2-ethylhexyl and 2-propylheptyl, dodecyl, tridecyl, myristyl, lauryl, i-C17, tall oil fat (C16,18), behenyl.
R2, R3 and R4, if present, are each more particularly and independently hydrogen, methyl, ethyl, propyl, butyl, pentyl and isobutyl, of which hydrogen, methyl and ethyl are particularly preferred and methyl and ethyl are very particularly preferred.
n is most preferably in the range from 3 to 20.
m is more preferably in the range from 3 to 20.
p is more preferably in the range from 3 to 20.
The sum total of n, m and p is more preferably in the range from 3 to 20. The individual alkoxide units can be arranged in various ways, for example randomly, in block form or with a gradient. Particular preference is given to processes first using a higher oxide, for example propylene oxide, and then EO.
In addition to various alkylene oxides, the process of the present invention may also utilize various alkoxylates a, b, c, ..., z being added at one or more times.
For instance, compounds where Ra = C12,14 to C2o and Rb = C2 to C10 may be used with advantage.
A useful base is in principle any compound capable of deprotonating the alkoxylate used. This includes bases within the meaning of Bjerrum's acid-base definition. There are certain preferred bases and hence a process wherein the base is selected from the group consisting of NaOH, KOH, Mg(OH)2, Ca(OH)2, ammonium hydroxide, choline hydroxide and hydrotalcite constitutes a particularly preferred embodiment of the present invention. Hydrotalcite is particularly preferred when the product is to have narrow molar mass distributions.
The base is added to the reaction mixture during the reaction either batchwise or continuously. This means that the base, or portions of the base, are added to the reaction mixture at a time at which reaction conditions are present.
A preferred embodiment is accordingly a process wherein the base is added to the reaction mixture at 2 to 10 000 times. The number of times at which the base is added is preferably in the range from 3 to 1000, more preferably in the range from 4 to 100 and most preferably in the range from 5 to 20.
Another preferred embodiment is a process wherein the base is added to the reaction mixture over a period of more than 30 minutes. The period over which the base is added to the reaction mixture is particularly advantageous in the range from more than 2 h to 10 h, preferably in the range from 5 h to 9 h and even more preferably in the range from 6 h to 8 h.
In both cases, i.e., in the case of the continuous addition of the base and in the case of the batchwise addition of the base, the base can be introduced into the reaction mixture at various places. It is particularly preferable when the base is added to the reactor at 2 to 10 places and preferably at 3 to 5 places. This procedure can be used to reduce the local concentration of base in the reaction mixture still further and thereby further suppress the formation of by-products.
As far as the catalyst is concerned, the metals of groups 4 to 12, i.e., from Ti to Zn and those thereunder, come into consideration as both main and secondary constituent, those of groups 8 to 11, i.e., Fe - Cu and those thereunder, being preferred.
And it is accordingly the case that a process wherein the transition metal catalyst comprises at least one metal selected from the group consisting of Fe, Cu, Co and Ni is preferred.
The transition metal can be in a variety of forms, such as pure metal or as metal oxide, but it is preferably present in activated form, as Raney metal. Raney copper is particularly preferred. This Raney copper can also be still further modified, for example by doping with other metals. It is an advantage of the process of the present invention that such doping is not needed to achieve a good result for the synthesis, but it may nevertheless be advantageous to further improve the result of the synthesis.
The preparation of suitable transition metal catalysts is described for example in EP 1 125 634 (Degussa), where a simple Raney copper fixed bed catalyst is disclosed.
EP 1 125 633 (Degussa) describes Raney copper comprising various dopants [example: 1 % Pt, 3% Fe, 2000 ppm Cr or 1 % V on Raney Cu], and it is shown that the doped catalysts deactivate less than conventional Raney copper (Degussa BFX
3113W). WO 96/01146 (Monsato) finally describes C support with a precious metal, for example Pt applied as anchor metal on the Cu. This technique is stated to likewise prevent the sintering of the Cu. A particularly preferred combination of transition metals is that of copper and iron. DMC catalysts are more particularly preferred.
The present process leaves only small amounts of catalyst in the product. In a preferred process the M content of the product is in the range from 0.1 ppm to 1%, preferably in the range from 1 to 500 ppm and more preferably in the range from 10 to 50 ppm.
The process of the present invention can pleasingly also be carried out on a large scale. Preference is accordingly given to a process utilizing more than 1 kg, preferably more than 10 kg, even more preferably more than 100 kg and most preferably more than 1 t (metric ton) of alkoxylate.
The process of the present invention wherein the reaction temperature is in the range from 140 C to 220 C is preferred. More preference is given to processes carried out in the temperature range from 160 to 200 C and more particularly in the range from 160 to 190 C, for example at 180 C.
The process of the present invention may in principle employ any solvent that is stable under the reaction conditions and does not react with the reactants or with the products. Preference is therefore given to solvents selected from the following list:
Name NMP
diethylene glycol dimethyl ether triethylene glycol dimethyl ether tetraethylene glycol dimethyl ether diethylene glycol diethyl ether 2- 2-metho ethox ethox acid sodium salt 2- 2- 2-methox ethox ethox etho acetic acid Decane Decalin Dodecane white oil 1,1,3,3-tetramethyl urea Tributylamine y-but rolactone Undecane tert-butylbenzene di ro l carbonate 2,5-dimethyl rrole 2,6-dimethylanisole 3,4-dimethylanisole 1,2-dimeth limidazole 4-ter-but l-1,2-dimeth (benzene And particular preference is given to the following solvents or suspension media:
N-methylpyrrolidone, triethylene glycol dimethyl ether, [2-(2-methoxyethoxy)ethoxy]
acid sodium salt and white oil.
There is also a preferred pressure range. Preference is given to a process wherein the pressure in the reaction vessel is less than 10 bar, preferably less than 5 bar and more preferably less than 2 bar. It is a particular advantage of the process of the present invention that it can also be carried out under atmospheric pressure, and that is in fact the most preferred embodiment.
Also protected are the ether carboxylates obtainable by this process and obtained by this process.
The use of these ether carboxylates in cleaning, crop protection and cosmetic applications and also as a solubilizer constitutes a further part of the subject matter of the present invention.
Compositions comprising ether carboxylates obtained by this process likewise form part of the subject matter of the present invention.
Further common constituents of compositions of this kind are mentioned in WO 2008/071582 for example.
The present invention is more particularly elucidated by the following examples, which do not restrict the scope of the invention:
Examples:
Example 1: Synthesis of nonionic ethoxylate (surfactant A) 10 300 g of a C12114 alcohol mixture of C8 < 0.3% by weight, C,o < 1.0% by weight, C12 > 65.0% by weight, C14 21.0% to 28.0% by weight, C16 4.0% to 8.0% by weight, < 0.5% by weight, for example Radianol C12-C161726 from Oleon, were initially charged with 2.6 g KOH (45% by weight in water) and dewatered together at 80 C and reduced pressure (about 20 mbar). Next 462 g of ethylene oxide were added by metered addition at 150 C and reacted at that temperature. The end of the reaction was determined via the drop in pressure. After purging with inert gas and cooling down to room temperature, the catalyst was neutralized by addition of 1.25 g of concentrated acetic acid.
Example 2: Oxidative dehydrogenation under atmospheric pressure in semi-batch process A 21 multi-neck flask equipped with internal thermometer, dropping funnel and distillation still head with column was initially charged with 498 g of surfactant A and also 30 g of Raney copper and the initial charge was heated to 180 C with stirring.
152 g of aqueous sodium hydroxide solution (25% strength) were added dropwise over a period of 8 h during which the water was distilled out of the reaction mixture. On completion of the addition of the aqueous sodium hydroxide solution the reaction mixture was stirred for a further 30 minutes. The reaction mixture was cooled down to 140 C and filtered through a frit and the effluent was analyzed.
Strong base titration:
7 mg KOH/g Weak base titration:
95 mg KOH/g OH number analysis:
reactant: 119 mg KOH/g effluent:13 mg KOH/g, corrected with strong base: 6 mg KOH/g; it follows that the conversion was 95%.
NMR (DMSO, CDCI3 = 1/1); 1H NMR, 13C decoupled:
6 = 0.85 (t, 3H, -CH3), 1.25 (s, 20H, CH2), 1.55 (m, 2H, -CH2CH2-O), 3.4 (m, 2H, CH2-O), 3.6 (m, 24H, O-CH2-CH2-O and CH2-OH of reactant), 3.75 (s, 1.77H, CH2-COO). It follows that the conversion was 89%.
HPLC: the sample was resolved in a system developed for the determination of free polyethylene glycol in nonionic surfactants. The principle of the analysis is that molecules having aliphatic moieties are retained on a reversed phase, whereas polar substances pass through the column without being retained. A switch valve was used to transfer the nonretarded fraction to a size exclusion column, on which the polymeric constituents were separated from low molecular weight secondary components.
The level of scissioning products in the analyzed sample was below 0.5 g/100 g.
Example 3: Oxidative dehydrogenation under superatmospheric pressure in batch process A 1.2 I autoclave with pressure maintenance at 15 bar was initially charged with 249 g of surfactant A together with 15 g of Raney copper (Degussa) and 76 g of aqueous sodium hydroxide solution (25%) and this initial charge was heated to 180 C
for 10 h with stirring. After removal of the catalyst by filtration, the organic phase was separated and titrated for weak base (6 mg KOH/g) and subjected to an OH number measurement (113 mg KOH/g) to determine conversion (6%).
Example 4: Oxidative dehydrogenation under superatmospheric pressure in semi-batch process A 1.2 I autoclave with pressure maintenance at 15 bar was initially charged with 249 g of surfactant A together with 15 g of Raney copper (Degussa) and this initial charge was heated to 180 C with stirring. In the course of 7 h, altogether 76 g of aqueous sodium hydroxide solution (25%) were metered into the autoclave using an HPLC
pump, followed by a further 30 minutes of stirring. After removal of the catalyst by filtration, the organic phase was separated and titrated for weak base (9 mg KOH/g) and subjected to an OH number measurement (115 mg KOH/g) to determine conversion (3.5%).
Name NMP
diethylene glycol dimethyl ether triethylene glycol dimethyl ether tetraethylene glycol dimethyl ether diethylene glycol diethyl ether 2- 2-metho ethox ethox acid sodium salt 2- 2- 2-methox ethox ethox etho acetic acid Decane Decalin Dodecane white oil 1,1,3,3-tetramethyl urea Tributylamine y-but rolactone Undecane tert-butylbenzene di ro l carbonate 2,5-dimethyl rrole 2,6-dimethylanisole 3,4-dimethylanisole 1,2-dimeth limidazole 4-ter-but l-1,2-dimeth (benzene And particular preference is given to the following solvents or suspension media:
N-methylpyrrolidone, triethylene glycol dimethyl ether, [2-(2-methoxyethoxy)ethoxy]
acid sodium salt and white oil.
There is also a preferred pressure range. Preference is given to a process wherein the pressure in the reaction vessel is less than 10 bar, preferably less than 5 bar and more preferably less than 2 bar. It is a particular advantage of the process of the present invention that it can also be carried out under atmospheric pressure, and that is in fact the most preferred embodiment.
Also protected are the ether carboxylates obtainable by this process and obtained by this process.
The use of these ether carboxylates in cleaning, crop protection and cosmetic applications and also as a solubilizer constitutes a further part of the subject matter of the present invention.
Compositions comprising ether carboxylates obtained by this process likewise form part of the subject matter of the present invention.
Further common constituents of compositions of this kind are mentioned in WO 2008/071582 for example.
The present invention is more particularly elucidated by the following examples, which do not restrict the scope of the invention:
Examples:
Example 1: Synthesis of nonionic ethoxylate (surfactant A) 10 300 g of a C12114 alcohol mixture of C8 < 0.3% by weight, C,o < 1.0% by weight, C12 > 65.0% by weight, C14 21.0% to 28.0% by weight, C16 4.0% to 8.0% by weight, < 0.5% by weight, for example Radianol C12-C161726 from Oleon, were initially charged with 2.6 g KOH (45% by weight in water) and dewatered together at 80 C and reduced pressure (about 20 mbar). Next 462 g of ethylene oxide were added by metered addition at 150 C and reacted at that temperature. The end of the reaction was determined via the drop in pressure. After purging with inert gas and cooling down to room temperature, the catalyst was neutralized by addition of 1.25 g of concentrated acetic acid.
Example 2: Oxidative dehydrogenation under atmospheric pressure in semi-batch process A 21 multi-neck flask equipped with internal thermometer, dropping funnel and distillation still head with column was initially charged with 498 g of surfactant A and also 30 g of Raney copper and the initial charge was heated to 180 C with stirring.
152 g of aqueous sodium hydroxide solution (25% strength) were added dropwise over a period of 8 h during which the water was distilled out of the reaction mixture. On completion of the addition of the aqueous sodium hydroxide solution the reaction mixture was stirred for a further 30 minutes. The reaction mixture was cooled down to 140 C and filtered through a frit and the effluent was analyzed.
Strong base titration:
7 mg KOH/g Weak base titration:
95 mg KOH/g OH number analysis:
reactant: 119 mg KOH/g effluent:13 mg KOH/g, corrected with strong base: 6 mg KOH/g; it follows that the conversion was 95%.
NMR (DMSO, CDCI3 = 1/1); 1H NMR, 13C decoupled:
6 = 0.85 (t, 3H, -CH3), 1.25 (s, 20H, CH2), 1.55 (m, 2H, -CH2CH2-O), 3.4 (m, 2H, CH2-O), 3.6 (m, 24H, O-CH2-CH2-O and CH2-OH of reactant), 3.75 (s, 1.77H, CH2-COO). It follows that the conversion was 89%.
HPLC: the sample was resolved in a system developed for the determination of free polyethylene glycol in nonionic surfactants. The principle of the analysis is that molecules having aliphatic moieties are retained on a reversed phase, whereas polar substances pass through the column without being retained. A switch valve was used to transfer the nonretarded fraction to a size exclusion column, on which the polymeric constituents were separated from low molecular weight secondary components.
The level of scissioning products in the analyzed sample was below 0.5 g/100 g.
Example 3: Oxidative dehydrogenation under superatmospheric pressure in batch process A 1.2 I autoclave with pressure maintenance at 15 bar was initially charged with 249 g of surfactant A together with 15 g of Raney copper (Degussa) and 76 g of aqueous sodium hydroxide solution (25%) and this initial charge was heated to 180 C
for 10 h with stirring. After removal of the catalyst by filtration, the organic phase was separated and titrated for weak base (6 mg KOH/g) and subjected to an OH number measurement (113 mg KOH/g) to determine conversion (6%).
Example 4: Oxidative dehydrogenation under superatmospheric pressure in semi-batch process A 1.2 I autoclave with pressure maintenance at 15 bar was initially charged with 249 g of surfactant A together with 15 g of Raney copper (Degussa) and this initial charge was heated to 180 C with stirring. In the course of 7 h, altogether 76 g of aqueous sodium hydroxide solution (25%) were metered into the autoclave using an HPLC
pump, followed by a further 30 minutes of stirring. After removal of the catalyst by filtration, the organic phase was separated and titrated for weak base (9 mg KOH/g) and subjected to an OH number measurement (115 mg KOH/g) to determine conversion (3.5%).
Claims (13)
1. A process for preparing an ether carboxylate of formula I
comprising reacting the corresponding compound of formula II
where independently R1 is a C1- to C50-alkyl, mono-, di-, tri-,...polyamine, X is O, COO, CH2-NH-O for q= 1 and r = 0 or N, N(CH2)t O for q = 2 and r = 0 to 50, R2 is H or C1- to C10-alkyl, R3 is H or C1- to C10-alkyl, R4 is H or C1- to C10-alkyl, M is H or a metal, ammonium or organic base, n is from 0 to 50, m is from 0 to 40, p is from 0 to 40, q is from 1 to 2, s is 0 or 1, t is from O to 20, provided that n + m + p is at least 1 and R is C1- to C50-alkyl, C1- to C50-alkenyl, C1- to C50-alkynyl, C6- to C50-aryl, C6- to C50-alkylaryl, H or a metal, preferably alkali, alkaline earth, with a base by using a transition metal catalyst which is present as Raney copper, the base being added to the reaction mixture continuously over a period above 30 minutes or discontinuously at two or more times.
comprising reacting the corresponding compound of formula II
where independently R1 is a C1- to C50-alkyl, mono-, di-, tri-,...polyamine, X is O, COO, CH2-NH-O for q= 1 and r = 0 or N, N(CH2)t O for q = 2 and r = 0 to 50, R2 is H or C1- to C10-alkyl, R3 is H or C1- to C10-alkyl, R4 is H or C1- to C10-alkyl, M is H or a metal, ammonium or organic base, n is from 0 to 50, m is from 0 to 40, p is from 0 to 40, q is from 1 to 2, s is 0 or 1, t is from O to 20, provided that n + m + p is at least 1 and R is C1- to C50-alkyl, C1- to C50-alkenyl, C1- to C50-alkynyl, C6- to C50-aryl, C6- to C50-alkylaryl, H or a metal, preferably alkali, alkaline earth, with a base by using a transition metal catalyst which is present as Raney copper, the base being added to the reaction mixture continuously over a period above 30 minutes or discontinuously at two or more times.
2. The process according to claim 1, wherein the compound of formula IV
where independently R is C1- to C50-alkyl, C1- to C50-alkenyl, C1- to C50-alkynyl, C6- to C50-aryl, C6- to C50-alkylaryl, H or a metal, X is O, COO, CH2-NH-O for q = 1 or N, N(CH2)t O for q = 2, R2 is H or C1- to C10-alkyl, R3 is H or C1- to C10-alkyl, R4 is H or C1- to C10-alkyl, M is H or a metal, ammonium or organic base, n is from 0 to 50, m is from 0 to 40, p is from 0 to 40, q is from 1 to 2, t is from 1 to 10, provided that n + m + p is at least 1, is reacted with a base by using a transition metal catalyst, the base being added to the reaction mixture continuously over a period above 30 minutes or discontinuously at two or more times.
where independently R is C1- to C50-alkyl, C1- to C50-alkenyl, C1- to C50-alkynyl, C6- to C50-aryl, C6- to C50-alkylaryl, H or a metal, X is O, COO, CH2-NH-O for q = 1 or N, N(CH2)t O for q = 2, R2 is H or C1- to C10-alkyl, R3 is H or C1- to C10-alkyl, R4 is H or C1- to C10-alkyl, M is H or a metal, ammonium or organic base, n is from 0 to 50, m is from 0 to 40, p is from 0 to 40, q is from 1 to 2, t is from 1 to 10, provided that n + m + p is at least 1, is reacted with a base by using a transition metal catalyst, the base being added to the reaction mixture continuously over a period above 30 minutes or discontinuously at two or more times.
3. The process according to claim 1 or 2, wherein the compound of formula VI
where independently R is C1- to C50-alkyl, C1- to C50-alkenyl, C1- to C50-alkynyl, C6- to C50-aryl, C6- to C50-alkylaryl, H or a metal, X is O, R2 is H or C1- to C10-alkyl, R3 is H or C1- to C10-alkyl, R4 is H or C1- to C10-alkyl, M is H or a metal, n is from 0 to 50, m is from 0 to 40, p is from 0 to 40, provided that n + m + p is at least 1, is reacted with a base by using a transition metal catalyst, the base being added added to the reaction mixture continuously over a period above 30 minutes or discontinuously at two or more times.
where independently R is C1- to C50-alkyl, C1- to C50-alkenyl, C1- to C50-alkynyl, C6- to C50-aryl, C6- to C50-alkylaryl, H or a metal, X is O, R2 is H or C1- to C10-alkyl, R3 is H or C1- to C10-alkyl, R4 is H or C1- to C10-alkyl, M is H or a metal, n is from 0 to 50, m is from 0 to 40, p is from 0 to 40, provided that n + m + p is at least 1, is reacted with a base by using a transition metal catalyst, the base being added added to the reaction mixture continuously over a period above 30 minutes or discontinuously at two or more times.
4. The process according to claim 2 or 3 wherein independently R is C1- to C50-alkyl, C1- to C50-alkenyl, C1- to C50-alkynyl, C6- to C50-aryl, C6- to C50-alkylaryl, H or a metal, X is O, COO, CH2-NH-O, N(CH2)t O
R2 is H or C2- to C8-alkyl, R3 is H or C2- to C8-alkyl, R4 is H or C2- to C8-alkyl, n is from 1 to 30, m is from 1 to 20, p is from 1 to 20, n + m + p is at least 2, t is an integer from 1 to 10.
R2 is H or C2- to C8-alkyl, R3 is H or C2- to C8-alkyl, R4 is H or C2- to C8-alkyl, n is from 1 to 30, m is from 1 to 20, p is from 1 to 20, n + m + p is at least 2, t is an integer from 1 to 10.
5. The process according to either of claims 2 and 3 wherein independently X is O or COO, R is C2- to C10-alkyl, R2 is H or C3- to C5-alkyl, R3 is H or C3- to C5-alkyl, R4 is H or C3- to C6-alkyl, n is from 1 to 18, m is from 1 to 12, m is from 1 to 12, n + m + p is at least 5.
6. The process according to any preceding claim wherein the base is selected from the group consisting of NaOH, KOH, Mg(OH)2, Ca(OH)2, ammonium hydroxide, choline hydroxide and hydrotalcite.
7. The process according to any preceding claim wherein the base is added to the reaction mixture at 2 to 10 000 times.
8. The process according to any preceding claim wherein the base is added to the reaction mixture over a period in the range from 2 to 10 hours.
9. The process according to any preceding claim wherein R is alkali or alkaline earth.
10. The process according to any preceding claim wherein M is alkali or alkaline earth.
11. The process according to any preceding claim wherein the transition metal catalyst is a Raney copper which is doped with other metals.
12. The process according to any preceding claim wherein the reaction temperature is in the range from 140°C to 220°C.
13. The process according to any preceding claim wherein the pressure in the reaction vessel is less than 10 bar.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10154070.6 | 2010-02-19 | ||
| EP10154070 | 2010-02-19 | ||
| PCT/EP2011/051993 WO2011101287A1 (en) | 2010-02-19 | 2011-02-10 | Method for the production of ether carboxylates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2787905A1 true CA2787905A1 (en) | 2011-08-25 |
Family
ID=44118861
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2787905A Abandoned CA2787905A1 (en) | 2010-02-19 | 2011-02-10 | Preparing ether carboxylates |
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| Country | Link |
|---|---|
| EP (1) | EP2536680B1 (en) |
| JP (1) | JP5905399B2 (en) |
| KR (1) | KR101794370B1 (en) |
| CN (1) | CN102762529B (en) |
| AU (1) | AU2011217344B2 (en) |
| BR (1) | BR112012019530A2 (en) |
| CA (1) | CA2787905A1 (en) |
| ES (1) | ES2554672T3 (en) |
| MX (1) | MX2012009294A (en) |
| MY (1) | MY156773A (en) |
| SG (1) | SG182613A1 (en) |
| WO (1) | WO2011101287A1 (en) |
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| JP2013519703A (en) * | 2010-02-19 | 2013-05-30 | ビーエーエスエフ ソシエタス・ヨーロピア | Method for producing ether carboxylate |
| US9062278B2 (en) | 2010-02-19 | 2015-06-23 | Basf Se | Preparing ether carboxylates |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2183853A (en) | 1934-12-22 | 1939-12-19 | Ig Farbenindustrie Ag | Polyoxyalkylene ether acid compounds containing a higher aliphatic group |
| US2384818A (en) | 1941-12-20 | 1945-09-18 | Carbide & Carbon Chem Corp | Preparation of amino carboxylic acids and their salts |
| US2384817A (en) | 1942-09-05 | 1945-09-18 | Carbide & Carbon Chem Corp | Catalytic alkaline oxidation of alcohols |
| US3717676A (en) | 1971-08-20 | 1973-02-20 | Air Prod & Chem | Synthesis of oxycarboxylic acid salts |
| US3799977A (en) * | 1972-01-28 | 1974-03-26 | Ici America Inc | Oxidation of glycols |
| JPS575775B2 (en) * | 1973-12-21 | 1982-02-01 | ||
| US3935257A (en) * | 1974-03-18 | 1976-01-27 | Monsanto Company | Chemical compounds |
| US4110371A (en) | 1975-11-04 | 1978-08-29 | Texaco Development Corporation | Preparation of oxydicarboxylic acid salts |
| DE3135946A1 (en) * | 1981-09-10 | 1983-03-24 | Bayer Ag, 5090 Leverkusen | Process for preparing alkoxyacetic acids |
| JP3129547B2 (en) * | 1992-11-18 | 2001-01-31 | 株式会社日本触媒 | Method for producing glycolate |
| EP0620209B1 (en) | 1993-04-12 | 1997-12-03 | Monsanto Company | Process to prepare carboxylic acid |
| US5916840A (en) | 1994-07-01 | 1999-06-29 | Monsanto Company | Process for preparing carboxylic acid salts and catalysts useful in such process |
| US5689000A (en) | 1994-07-01 | 1997-11-18 | Monsanto Company | Process for preparing carboxylic acid salts and catalysts useful in such process |
| EP0946295B1 (en) | 1996-09-26 | 2003-12-03 | Akzo Nobel N.V. | Catalyst for dehydrogenation of amino alcohols to amino carboxylic acids or of ethylene glycol (derivatives) to oxycarboxylic acids, method for their production and their use |
| JP3886201B2 (en) | 1997-04-07 | 2007-02-28 | 川研ファインケミカル株式会社 | Ultra fine powder copper catalyst, carboxylate and alkyl ether carboxylate type anionic surfactant using the catalyst |
| ITTO980249A1 (en) * | 1998-03-23 | 1999-09-23 | Finchimica Srl | PROCEDURE FOR THE PREPARATION OF SALTS OF CARBOXYLIC ACIDS |
| TR200103150T2 (en) * | 1999-05-03 | 2002-03-21 | Monsanto Technology Llc | Preparation of carboxylic acid salts from primary alcohols |
| EP1382595A1 (en) | 2000-02-18 | 2004-01-21 | Degussa AG | Fixed bed copper Raney catalyst for dehydrogenating alcohols |
| ATE350158T1 (en) * | 2000-02-18 | 2007-01-15 | Degussa | METHOD FOR PRODUCING CARBOXYLIC ACIDS BY DEHYDRATION OF ALCOHOLS |
| EP1382389A1 (en) * | 2000-02-18 | 2004-01-21 | Degussa AG | Raney copper catalyst for the dehydrogenation of alcohols |
| CN1729052A (en) | 2001-10-18 | 2006-02-01 | 孟山都技术公司 | Process and catalyst for dehydrogenating primary alcohols to make carboxylic acid salts |
| DE10161674A1 (en) * | 2001-12-14 | 2003-06-26 | Basf Ag | Catalysts for the production of carboxylic acid salts from alcohols, useful as chelates in detergents and pharmaceuticals, comprise copper and are prepared by precipitation of copper salt solutions with a base and reduction with hydrogen |
| JP5366821B2 (en) | 2006-12-14 | 2013-12-11 | ビーエーエスエフ ソシエタス・ヨーロピア | Nonionic emulsifiers for emulsion concentrates for spontaneous emulsification |
| JP2013519703A (en) * | 2010-02-19 | 2013-05-30 | ビーエーエスエフ ソシエタス・ヨーロピア | Method for producing ether carboxylate |
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- 2011-02-10 WO PCT/EP2011/051993 patent/WO2011101287A1/en active Application Filing
- 2011-02-10 KR KR1020127024331A patent/KR101794370B1/en active IP Right Grant
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- 2011-02-10 MX MX2012009294A patent/MX2012009294A/en unknown
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- 2011-02-10 SG SG2012053476A patent/SG182613A1/en unknown
- 2011-02-10 CN CN201180009831.XA patent/CN102762529B/en not_active Expired - Fee Related
- 2011-02-10 EP EP11702838.1A patent/EP2536680B1/en not_active Not-in-force
- 2011-02-10 BR BR112012019530-1A patent/BR112012019530A2/en not_active Application Discontinuation
- 2011-02-10 AU AU2011217344A patent/AU2011217344B2/en not_active Ceased
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| MY156773A (en) | 2016-03-31 |
| WO2011101287A1 (en) | 2011-08-25 |
| ES2554672T3 (en) | 2015-12-22 |
| JP2013519700A (en) | 2013-05-30 |
| CN102762529A (en) | 2012-10-31 |
| AU2011217344B2 (en) | 2016-03-24 |
| SG182613A1 (en) | 2012-09-27 |
| KR20130023204A (en) | 2013-03-07 |
| MX2012009294A (en) | 2012-09-07 |
| EP2536680A1 (en) | 2012-12-26 |
| KR101794370B1 (en) | 2017-11-06 |
| EP2536680B1 (en) | 2015-09-02 |
| JP5905399B2 (en) | 2016-04-20 |
| AU2011217344A1 (en) | 2012-09-06 |
| BR112012019530A2 (en) | 2018-03-13 |
| CN102762529B (en) | 2016-12-21 |
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